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nsv5491842

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:141,073

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 982 SVs from 73 studies. See in: genome view    
Submitted genomic142,196,282-142,337,354Question Mark
Overlapping variant regions from other studies: 982 SVs from 73 studies. See in: genome view    
Remapped(Score: Perfect):143,277,643-143,418,715Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5491842Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8142,196,282142,337,354
nsv5491842RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8143,277,643143,418,715

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17019272deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17019272Submitted genomicNC_000008.11:g.142
196282_142337354de
l
GRCh38 (hg38)NC_000008.11Chr8142,196,282142,337,354
nssv17019272RemappedPerfectNC_000008.10:g.143
277643_143418715de
l
GRCh37.p13First PassNC_000008.10Chr8143,277,643143,418,715

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17019272<0.00116404
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